8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
DMS-9000
FDA 510(k)
FDA Class 1
·General Hospital
VERTE-STACK® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074019345·SPACER 2960836 CAPS VS PEEK VBS END 36X8
VISTADENT OC - VERSION 4
FDA 510(k)
FDA Class 2
·Radiology
Menai System
FDA 510(k)
FDA Class 2
·Anesthesiology
BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024
REPAIR NEPTUNE 2 ROVER
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code FYD·December 17, 2010
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·January 11, 2013
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW·Product code NXT·July 28, 2014